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Lab Tech - II

Job in Waldorf, Charles County, Maryland, 20602, USA
Listing for: Spectraforce Technologies
Full Time position
Listed on 2026-01-11
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Job Description & How to Apply Below

Job Title - Quality Control Technician I (QC Lab Support) Work Arrangement

Fredrick, MD 21704, 100% Onsite (Laboratory Environment)

Shift & Schedule
  • Day Shift: 4 days O 10 hours
  • Sunday - Wednesday | 7:00 AM - 6:00 PM
Duration

12 Months

Role Overview

The Quality Control Technician I - QC Lab Support is responsible for executing activities related to sample management, sample shipment, and laboratory support within the QC function. This role requires close cross-functional collaboration with Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), Corporate QC
, and other QC teams to ensure compliant and efficient laboratory operations.

Key Responsibilities
  • Receive incoming samples, verify documentation, and log sample information into LIMS
    .
  • Support sample receipt, processing, and aliquoting for release, stability testing, and retain samples.
  • Label, store, organize, and maintain samples according to established procedures and storage requirements.
  • Coordinate sample transfers to internal and external testing laboratories.
  • Perform routine cleaning, maintenance, and restocking of sample storage areas.
  • Collaborate with MM, QA, and QC functions
    , including Corporate QC, to support sampling, testing, and disposition activities.
  • Manage and complete shipping activities within QC functions.
  • Review and complete documentation, including chain-of-custody forms, processing logs, logbooks
    , and other QC records.
  • Assist with deviations and investigations as needed.
  • Provide updates during daily and weekly meetings
    .
  • Participate in Lean Lab and other Operational Excellence initiatives.
  • Ensure compliance with all safety, quality, and regulatory guidelines.
  • Perform additional duties as assigned.
Basic Qualifications
  • Bachelor's Degree
    , OR
  • Associate's Degree with 2+ years of experience in Quality Control or biopharma laboratories (FDA-regulated preferred), OR
  • High School Diploma with 3+ years of experience in Quality Control or biopharma laboratories (FDA-regulated preferred).
Preferred Qualifications
  • Strong knowledge of GMP application in a QC laboratory environment.
  • Exceptional attention to detail and ability to manage multiple priorities.
  • Proficiency in Microsoft Office
    , Excel
    , Visio
    , and related applications.
  • Excellent interpersonal, verbal, and written communication skills in a collaborative environment.
  • Comfortable working in a fast-paced
    , small company environment with shifting priorities.
  • Flexible with schedule and willing to work overtime as needed
    .
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